Hydroquinone ether compounds

ABSTRACT

New hydroquinone ether compounds of formula I are described: ##STR1## wherein p is 1 or 2 and q is 0 or 1, provided that p+q is 1 or 2, R is a residue of formula II ##STR2## and R o , R oo , R 1 , R 2 , R 3 , Q, n and k are as defined in the specification. 
     The new compounds are useful e.g. as stabilizers in photographic material.

This application is a division of application Ser. No. 504,283, filed June 14, 1983 (now U.S. Pat. No. 4,549,015).

The present invention relates to new hydroquinone compounds, especially functionally alkylated hydroquinone ethers useful in photographic systems.

Hydroquinone derivatives containing functional groups are described for example in the GB-patent specification No. 1 465 082 (monoalkylated hydroquinone compounds) and in the JP-patent application publication No. 54/73032 (hydroquinone diethers).

According to the present invention, there are provided compounds having the formula I ##STR3## wherein p is 1 or 2 and q is 0 or 1, provided that p+q is 1 or 2; R is a residue of formula II ##STR4## wherein Q is selected from the residues:

(i) --COZR₄ wherein Z is --O-- or --NR₅, and R₄ independently is H, a C₁ -C₂₀ straight or branched chain alkyl optionally interrupted by 1 to five oxygen atoms and optionally substituted by a group --OR₆ wherein R₆ is C₃ -C₁₂ cycloalkyl, straight or branched C₃ -C₂₀ alkenyl, C₆ -C₁₀ aryl optionally substituted by one or two C₁ -C₄ alkyl groups, or C₇ -C₁₃ aralkyl, or R₄ is a divalent C₂ -C₂₀ straight or branched chain alkylene residue, a C₃ -C₂₀ straight or branched chain alkenyl group or a C₃ -C₁₂ cycloalkyl group; a C₆ -C₁₀ aryl group optionally substituted by one or two C₁ -C₈ alkyl groups or a C₇ -C₁₃ aralkyl group; a 5 or 6 membered heterocycle containing an oxygen atom, and optionally substituted by one or two C₁ -C₄ straight or branched chain alkyl groups; or methyl substituted by a 5 or 6 membered heterocycle containing an oxygen atom and optionally substituted by one or two C₁ -C₄ straight or branched chain alkyl groups; and when Z is --NR₅, R₅ is hydrogen, a C₁ -C₂₀ straight or branched chain alkyl group, or a C₅ -C₆ cycloalkyl group, or R₄ and R₅, together with the nitrogen atom to which they are each bonded, may form a 5 or 6 membered heterocyclic ring, optionally substituted by one or two C₁ -C₄ alkyl groups;

(ii) --OX wherein X is R₇ or --COR₇, wherein R₇ is --H or a C₁ -C₂₀ straight or branched chain alkyl group, a C₃ -C₂₀ straight or branched chain alkenyl group, a C₃ -C₁₂ cycloalkyl group, a C₇ -C₁₃ aralkyl group, or a C₆ -C₁₀ aryl group, optionally substituted by one or two C₁ -C₄ alkyl groups;

(iii) --N(R₈)(R₉) wherein R₈ and R₉ independently are --H or a C₁ -C₂₀ straight or branched chain alkyl group, a C₃ -C₂₀ straight or branched chain alkenyl group, a C₃ -C₁₂ cycloalkyl group, a C₇ -C₁₃ aralkyl group, or a C₆ -C₁₀ aryl group optionally substituted by one or two C₁ -C₄ alkyl groups, or R₉ is an acyl group of formula --COR₇ wherein R₇ has its previous significance, or R₈ and R₉, together with the nitrogen atom to which they are each bonded, form a 5- or 6-membered heterocyclic ring, optionally substituted by one or two C₁ -C₄ alkyl groups;

(iv) --PO(OR₁₀) ([0]_(x) R₁₁) wherein x is 0 or 1, and when x is 1 R₁₀ and R₁₁ are the same or different and each is --H or a C₁ -C₂₀ straight or branched chain alkyl group or a C₆ -C₁₀ aryl group optionally substituted with one or two C₁ -C₄ alkyl groups; or R₁₀ and R₁₁ may be linked together to form a C₂ -C₃ alkylene chain optionally substituted by one to four C₁ -C₂₀ alkyl groups; and when x is 0, R₁₀ has its previous significance and R₁₁ is a C₁ -C₅ straight chain alkyl group;

(v) --SO₂ R₁₂ wherein R₁₂ is --OH, --Cl or --N(R₅)(R₇) wherein R₅ and R₇ have their previous significance; provided that, when R₁₂ is --OH, then R₁ is a residue of formula II;

(vi) --CN, halogen or --NO₂ ; and

(vii) --COR₁₅ wherein R₁₅ is --H or a C₁ -C₂₀ straight or branched alkyl group or halogen;

n is an integer from 1 to 20; k is 1 or 2; R₂ and R₃ are the same or different and each is straight or branched chain alkyl group having from 1 to 5 carbon atoms and, when Q is --CO₂ R₄, either R₂ or R₃ is optionally substituted by a --CO₂ R₄ group, the R₄ groups being independent, or when Q is --COOR₄ R₂ or R₃ may be so linked to the residue C_(n) H_(2n) --COOR₄ that there is formed a C₅ -C₁₂ cycloalkylene residue optionally substituted by another group --CO₂ R₄, the R₄ groups being independent, wherein R₄ has its previous significance, or when Q is --COR₁₅ R₂ or R₃ may be so linked to the residue C_(n) H_(2n) --COR₁₅ that there is formed a C₅ -C₁₂ cycloalkylene residue wherein R₁₅ has its previous significance, provided that, when the group Q is a --CO₂ R₄ residue wherein R₄ is a divalent C₂ -C₂₀ straight or branched chain alkylene residue, then p and k are both 1 and the compound of formula I has the formula Ia: ##STR5## wherein R₄₀ is a C₂ -C₂₀ divalent straight or branched chain alkylene residue; and provided that, when the group Q is a --CON(R₄)(R₅) residue wherein R₄ is a C₂ -C₂₀ divalent straight or branched chain alkylene residue and R₅ has its previous significance, then p and k are both 1 and the compound of formula I has the formula Ib: ##STR6## wherein R₂, R₃, q and n have their previous significance, R₄₁ is a C₂ -C₂₀ divalent straight or branched chain alkyl residue; R₁ is C₁ -C₈ straight or branched chain alkyl, C₅ -C₇ cycloalkyl optionally substituted by one or two methyl or ethyl groups, C₇ -C₉ aralkyl or a residue of formula II as hereinbefore define, and when R₁ is a residue of formula II then R₁ and R may be the same or different; or R₁ is a residue of formula III: ##STR7## in which R and p have their previous significance; and M is a direct bond, --C(R₁₃)(R₁₄)-- in which R₁₃ and R₁₄ are the same or different and are hydrogen, C₁ -C₂₀ straight or branched chain alkyl optionally interrupted by 1 to 3 sulphur atoms, C₆ -C₁₀ aryl or R₁₃ and R₁₄, together with the carbon atom to which they are attached may form a 5- or 6-membered ring which may be further substituted by one or two C₁ -C₈ straight or branched chain alkyl groups; --S--; --S--S--; --SO₂ --; --CH₂ SCH₂ --; --CH₂ OCH₂ -- or --C(CH₃)₂ -p-phenylen-C(CH₃)₂ --; R_(o) and R_(oo) are the same or different and each is hydrogen, a C₁ -C₂₀ straight or branched chain alkyl group optionally interrupted by 1 to 5 oxygen atoms, a cycloalkyl group having 3 to 12 carbon atoms, a C₆ -C₁₀ aryl group optionally substituted by one or two C₁ -C₄ straight or branched chain alkyl groups or a C₇ -C₁₃ aralkyl group provided that R_(o) and R_(oo) are not both hydrogen, or R_(oo) has its previous significance and R_(o) is a residue of formula IV ##STR8## in which R, R_(oo), R₁ and q have their previous significance, or R_(o) and R₁ when in ortho-position to one another, together with the carbon atoms to which they are attached may form an optionally substituted residue of formula V ##STR9## wherein A is a carbon residue containing 4 to 20 carbon atoms which forms a substituted chroman or coumaran system, or R_(o) and R₁ together may form a residue having the formula VI or VII: ##STR10## wherein R, R_(o) and R_(oo) have their previous significance, provided that the compound of formula I contains only one residue of formula III or IV; or R_(oo) is hydrogen and R_(o) is a residue having the formula IVa or IVb: ##STR11## wherein p, q and R have their previous significance, R₁ " is C₁ -C₈ straight or branched alkyl, C₇ -C₉ aralkyl or a residue of formula II, as hereinbefore defined, m is 1 or 2, B, when m is 1, represents C₂ -C₁₂ alkylene which may be interrupted by 1 to 3 oxygen or sulphur atoms, C₄ -C₁₀ alkenylene, C₅ -C₁₂ cycloalkylene, C₆ -C₁₂ arylene, C₈ -C₁₂ aralkylene, C₄₋₆ alkynylene, xylylene, --CH₂ CH(OH)CH₂ --, --CH₂ CH(OH)CH₂ --O--Y--O--CH₂ CH(OH)CH₂ --, ##STR12## or --CH₂ COO--B'--OCOCH₂ -- wherein Y is C₂ -C₁₀ alkylene, C₆ -C₁₂ arylene, ##STR13## or C₆ -C₁₂ cycloalkylene, B' is C₂ -C₈ alkylene, C₄ -C₈ oxaalkylene, or cyclohexylene and, when m is 2, B represents a group of the formula ##STR14## r is 0 to 12, preferably 0, R₁₆ represents hydrogen or straight or branched C₁ -C₁₂ alkyl and D is --OR₄ or --N(R₄)(R₅) wherein R₄ and R₅ have their previous significance; as well as salts of compounds of formula I with bases or organic or inorganic acids, respectively, when Q is an acidic or basic group.

When the group R₁ is a C₁ -C₈ straight or branched chain alkyl group it may be, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, iso-butyl, t-butyl, t-pentyl or 1,1,3,3-tetramethylbutyl.

When the group R₂ or R₃ is a C₁ -C₅ straight or branched chain alkyl group it may be, for example, a methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, n-pentyl or neopentyl group.

When the group R₄, R_(o) or R_(oo) is a C₁ -C₂₀ straight or branched chain alkyl group optionally interrupted by one to 5 oxygen atoms it may be, for example, a methyl, ethyl, 2-methoxyethyl, 2-ethoxyethyl, 2-n-propoxyethyl, 2-n-butoxyethyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, n-dodecyl, n-tetradecyl, n-hexadecyl, n-octadecyl, n-eicosyl, --(C₂ H₄ O)₂ CH₃, --(C₂ H₄ O)₃ CH₃, --(C₂ H₄ O)₄ CH₃ or --(C₂ H₄ O)₅ CH₃ group.

When R₄, R₆, R₇, R₈ or R₉ is a C₃ -C₂₀ straight or branched chain alkenyl group, it may be for example, a prop-2-enyl, n-but-2-enyl, 2-methyl-prop-2-enyl, n-pent-2-enyl, n-hex-2-enyl, n-hexa-2,4-dienyl, n-dec-10-enyl, or n-eicos-2-enyl group.

When the group R₄, R₆, R₇, R₈, R₉, R_(o) or R_(oo) is a C₃ -C₁₂ cycloalkyl group, it may be, for example, a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclooctyl, cyclodecyl, adamantyl, or cyclododecyl group. When the group R₅ is a C₅ -C₆ cycloalkyl group it may be a cyclopentyl or cyclohexyl group. When the group R₄, R₆, R₇, R₈, R₉, R_(o) or R_(oo) is a C₇ -C₁₃ aralkyl group it may be, for example, a benzyl, phenylethyl, benzhydryl, or naphthylmethyl group. When the group R₁ is a C₇ -C₉ aralkyl group, it may be e.g. a cumyl group. When the group R₄ is a C₆ -C₁₀ aryl group optionally substituted by one or two C₁ -C₈ -straight or branched chain alkyl groups, it may be a phenyl, tolyl, xylyl, cumyl, butylphenyl, phenyl substituted by 1 or 2 1,1,3,3-tetramethylbutyl groups or naphthyl group.

When the group R₆, R₇, R₈, R₉, R₁₀, R₁₁, R_(o) or R_(oo) is a C₆ -C₁₀ aryl group optionally substituted by one or two C₁ -C₄ straight or branched chain alkyl groups, it may be, a phenyl, tolyl, xylyl, cumyl, butylphenyl or naphthyl group.

When the group R₄ is a 5- or 6-membered heterocycle containing oxygen, and optionally substituted by one or two straight or branched chain C₁ -C₄ alkyl groups, it may be, for example, tetrahydrofuran-3-yl, tetrahydropyran-4-yl or 2,6-dimethyl-tetrahydropyran-4-yl. When the group R₄ is methyl substituted by a 5- or 6-membered heterocycle containing an oxygen atom, and optionally substituted by one or two straight or branched chain C₁ -C₄ alkyl groups, it may be, for example, furfuryl, tetrahydrofurfuryl or tetrahydropyran-2-yl-methyl.

When the groups R₄ and R₅, and the groups R₈ and R₉, together with the nitrogen atom to which they are bonded form a 5- or 6-membered heterocyclic ring, optionally substituted by one or two C₁ -C₄ alkyl groups, this ring may be for example a pyrrolidine, piperidine, morpholine or a 2,5-dimethyl morpholine ring.

When the groups R₅, R₇, R₈, R₉, R₁₀, R₁₁, R₁₃, R₁₄, R₁₅, R_(o) or R_(oo) are C₁ -C₂₀ straight or branched chain alkyl they may be the same or different and may be methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, n-dodecyl, n-tetradecyl, n-hexadecyl, n-octadecyl or n-eicosyl groups. Preferred alkyl groups R_(o) and R_(oo) are those containing 1 to 8 carbon atoms, optionally interrupted by 1 or 2 oxygen atoms.

When the groups R₁₀ and R₁₁ are linked to form a C₂ -C₃ methylene chain optionally substituted by one to four C₁ -C₂₀ alkyl chains, they may be for example --CH₂ CH₂ --, --CH₂ --CH₂ --CH₂ --, --CH₂ CH(CH₃)--, --CH₂ CH(C₂ H₅)--, --CH₂ CH(C₂₀ H₄₁)--, --CH(CH₃)CH(CH₃)--, --CH(CH₃)C(CH₃)₂ --, --C(CH₃)₂ C(CH₃)₂ --, --CH₂ CH₂ --C(CH₃)₂ --, or --CH(CH₃)CH₂ CH(CH₃)-- groups.

When the groups R₁₃ and R₁₄ are linked to form a C₄ - or C₅ -alkylene chain optionally substituted by one or two C₁ -C₈ alkyl chains, they may be e.g. --(CH₂)₄ --, --(CH₂)₅ --, --CH₂ CH₂ --C(CH₃)--CH₂ CH₂ --, --CH₂ CH₂ --CH(t--C₄ H₉)--CH₂ CH₂ -- or --CH₂ CH₂ CH(CH₃)CH₂ CH(CH₃)--.

When the groups R_(o) and R, together with the ring to which they are attached, form a substituted chroman or coumarin ring, they may be e.g. a 2,2,4-trimethyl- or 2,2-dimethyl-4-isopropyl chroman or 2,2-dimethyl-coumaran.

When the group B is a C₂ -C₂₂ alkylene chain optionally interrupted by one to three O- or S-atoms it may be e.g. --(CH₂)₂ --, --(CH₂)₃ --, --(CH₂)₄ --, --(CH₂)₆ --, --(CH₂)₈ --, --(CH₂)₁₀ --, --(CH₂)₁₆ --, --(CH₂)₂₂ --, --CH₂ CH₂ OCH₂ CH₂ --, --CH₂ CH₂ (OCH₂ CH₂)₂ --, --CH₂ CH₂ (OCH₂ CH₂)₃ -- or --CH₂ CH₂ SCH₂ CH₂ --.

When the group B is a C₄ -C₁₀ alkenylene chain it may be e.g. --CH₂ CH═CH--CH₂ --, --CH₂ CH═CH--CH═CH--CH₂ --, --(CH₂)₄ CH═CH(CH₂)₄ --.

When the group B is a C₅ -C₈ cycloalkylene group it may be e.g. 1,1-cyclohexylene, 1,2-cyclohexylene or 1,4-cyclohexylene.

When the groups B and Y are C₆ -C₁₂ arylene they may be e.g. a 1,2-phenylene, 1,4-phenylene, or 4,4'-biphenylene.

When the group B is a C₈ -C₁₂ aralkylene it may be e.g. ##STR15##

When the group B is a C₄ -C₆ alkynylene it may be for example --CH₂ --C.tbd.C--CH₂ --, or --C.tbd.C--C.tbd.C--.

When the group Y is a C₂ -C₁₀ alkylene, it may be e.g. --(CH₂)₂ --, --(CH₂)₃ --, --(CH₂)₄ --, --(CH₂)₆ --, --(CH₂)₈ -- or --(CH₂)₁₀ --.

When the group Y is a C₅ -C₁₂ cycloalkylene it may be e.g. 1,2-cyclohexylene, 1,3-cyclohexylene, 1,4-cyclohexylene, 1,2-cyclooctylene or 1,2-cyclododecylene.

When the group B' is a C₂ -C₈ alkylene it may be e.g. --(CH₂)₂ --, --(CH₂)₃ --, --(CH₂)₄ --, --(CH₂)₆ -- or --(CH₂)₈ --.

When the group B' is a C₄ -C₈ oxaalkylene group it may be e.g. --CH₂ CH₂ OCH₂ CH₂ --, or --CH₂ CH₂ (OCH₂ CH₂)₃ --.

When the group R₁₆ is a C₁ -C₁₂ straight or branched chain alkyl group it may be, methyl, ethyl, n-propyl, isopropyl, butyl, sec.-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl or n-dodecyl group.

When the group R₁₅ or Q is a halogen it may be fluorine, chlorine or bromine.

Examples of salts where Q is an acidic group e.g. --COOH include salts with alkali and alkaline earth metals and amines and, where Q is a --N(R₈)(R₉) group, salts with organic and inorganic acids, for example, hydrochloric-, sulphuric-, para-toluene-sulphonic- and oxalic acids.

In one preferred embodiment, the groups R and R₁ are bonded in the 2- and 5-positions, respectively, in the hydroquinone ethers of formula I. Other preferred compounds of the invention are those having the formula VIII: ##STR16## wherein R₂, R₃, R_(o), R_(oo), n, k and Q have their previous significance and R₁ is a group of formula II as hereinbefore defined, or is a group of formula IX: ##STR17## wherein G is C₁ -C₅ alkyl or phenyl as well as salts thereof.

Preferred compounds of formula VIII and their salts are those wherein R₁ is a group of formula II or IX, Q is --COZR₄ or --OR₇ in which Z, R₄, R₅ and R₇ have their previous significance, R₂ and R₃, independently, are methyl, ethyl, n-propyl, isopropyl or neopentyl; or either R₂ or R₃ is optionally substituted by a group --COOR₄ wherein R₄ has its previous significance, or R₂ or R₃ may be so linked to the residue C_(n) H_(2n) --COOR₄ that there is formed a cycloalkylene residue having 5 to 8 carbon atoms which is substituted by another --COOR₄ ; and R_(o), R_(oo), n and k have their previous significance; more particularly compounds of formula VIII wherein k is 1, R₁ is a group of formula II or IX, Q is --COZR₄ or --OR₅, n is an integer from 1 to 10, R₂ and R₃, independently, are methyl, ethyl or neopentyl, or one of R₂ and R₃ may be so linked to the residue --C_(n) H_(2n) --COOR₄ that there is formed a cyclohexylene residue which is substituted by --COOR₄, R₄ is hydrogen, C₁₋₂₀ alkyl, optionally interrupted by 1, 2 or 3 oxygen atoms and/or optionally substituted by --OR₆ wherein R₆ is cyclopentyl, cyclohexyl, cyclooctyl, C₃ -C₁₀ alkenyl, phenyl, benzyl, phenethyl, benzhydryl or naphthylmethyl, or R₄ is C₃ -C₁₅ alkenyl or phenyl optionally substituted by 1 or 2 C₁ -C₄ alkyl groups, benzyl, phenethyl, cyclopentyl, cyclohexyl or a 5- or 6-membered heterocyclic ring containing an oxygen atom, which ring is optionally substituted by 1 or 2 C₁ -C₄ alkyl groups, and Z, R_(o), R_(oo) and R₇ have their previous significance, or R₄ and R₅, together with the nitrogen atom to which they are each bonded, form a 5- or 6-membered heterocyclic ring, optionally substituted by one or two C₁ -C₄ alkyl groups: as well as salts of these compounds.

Still further preferred compounds of formula VIII wherein k is 1, R₁ is a group of formula II or IX, Q is --COZR₄ or --OR₇, and their salts, are those wherein Z has its previous significance, n is an integer from 1 to 10, R₂ and R₃, independently, are methyl, ethyl or neopentyl, or one of R₂ and R₃ may be so linked to the residue --C_(n) H_(2n) --COOR₄ that there is formed a cyclohexylene residue which is substituted by --COOR₄, R₄ is C₁ -C₂₀ alkyl optionally interrupted by 1 or 2 oxygen atoms and/or optionally substituted by cyclohexyloxy, C₃ -C₁₀ alkenyloxy, phenoxy or benzyloxy, or R₄ is C₃ -C₁₅ alkenyl, phenyl, benzyl, phenylethyl, cyclopentyl, cyclohexyl, a 5- or 6-membered heterocyclic ring containing an oxygen atom, or methyl substituted by a 5- or 6-membered heterocyclic ring containing an oxygen atom, and is especially C₁ -C₁₆ alkyl optionally interrupted by an oxygen atom, or optionally substituted by phenoxy, or R₄ is C₃ -C₁₅ alkenyl, phenyl, benzyl, tetrahydrofuran-3-yl or tetrahydrofurfuryl, R₇ is hydrogen or C₁ -C₁₅ alkyl, or R₄ and R₅, together with the nitrogen atom to which they are each bonded, form a 5- or 6-membered heterocyclic ring optionally substituted by one or two C₁ -C₄ alkyl groups, and R_(o) and R_(oo) are hydrogen or C₁ -C₈ alkyl, optionally, but preferably not, interrupted by 1 or 2 oxygen atoms, cyclohexyl, phenyl or benzyl, or R_(o) and R₁ together form a residue of formula V as hereinbefore defined.

Particularly preferred compounds of formula VIII and their salts are those wherein k is 1, R₁ is a group of formula II or IX, Q is --COZR₄ or --OR₇ wherein Z has its previous significance, n is an integer from 1 to 3, R₂ and R₃ are each methyl or neopentyl, R₄ is C₁ -C₁₆ alkyl optionally interrupted by an oxygen atom or optionally substituted by phenoxy, or R₄ is C₃ -C₁₅ alkenyl, phenyl, benzyl, tetrahydrofuran-3-yl or tetrahydrofurfuryl, R₇ is hydrogen or C₁ -C₁₅ alkyl or R₄ and R₅, together with the nitrogen atom to which they are each bonded, form a 5- or 6-membered heterocyclic ring optionally substituted by one or two C₁ -C₄ alkyl groups, and R_(o) and R_(oo) are hydrogen or C₁ -C₄ alkyl, or R_(o) and R₁ together form a residue of formula V as hereinbefore defined, provided that when Q is --OR₇, R₇ is, in particular, C₁ -C₈ alkyl.

Preferably, one of R_(o) and R_(oo) is hydrogen and the other is C₁ -C₄ alkyl, or R_(o) and R₁ together form a residue of formula V as hereinbefore defined.

Non-limiting examples of Compounds of Formula I include:

2-(3'-methoxycarbonyl-2'-methyl-prop-2'-yl)-4-methoxyphenol

2-(3'-n-hexyloxycarbonyl-2'-methyl-prop-2'-yl)-4-methoxyphenol

5-t-butyl-2-(3'-n-hexyloxycarbonyl-2'-methyl-prop-2'-yl)-4-methoxyphenol

5-t-butyl-2-(3'-n-dodecyloxycarbonyl-2'-methyl-prop-2'-yl)-4-methoxyphenol

2,5-bis-(3'-methoxycarbonyl-2'-methyl-prop-2'-yl)-4-methoxyphenol

2,5-bis-(3'-n-hexyloxycarbonyl-2'-methyl-prop-2'-yl)-4-methoxyphenol

2,5-bis-(3'-n-dodecyloxycarbonyl-2'-methyl-prop-2'-yl)-4-methoxyphenol

2-(4'-methoxycarbonyl-1'-methyl-cyclohex-1'-yl)-4-methoxyphenol

2-(4'-n-hexyloxycarbonyl-1'-methyl-cyclohex-1'-yl)-4-methoxyphenol

2,5-bis-(4'-methoxycarbonyl-1'-methyl-cyclohex-1'-yl)-4-methoxyphenol

2,5-bis-(4'-n-hexyloxycarbonyl-1'-methyl-cyclohex-1'-yl)-4-methoxyphenol

2,5-bis-(3',4'-bis-methoxycarbonyl-1'-methyl-cyclohex-1'-yl)-4-methoxyphenol

2 and 3-(3',4'-bis-methoxycarbonyl-cyclohex-1'-yl)-4-methoxyphenol

2 and 3-(4'-acetyl-1'-methyl-cyclohex-1'-yl)-4-methoxyphenol

2 and 3-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-methyl-4-methoxyphenol

5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2-methyl-4-methoxyphenol

5-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-2-t-butyl-4-methoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-t-butyl-4-methoxyphenol

5-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-2-t-butyl-4-methoxyphenol

5-(5'-n-dodecyloxycarbonyl-2'-methyl-pent-2'-yl)-2-t-butyl-4-methoxyphenol

5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2-(1',1',3',3'-tetramethylbutyl)-4-methoxyphenol

2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-5-(1',1',3',3'-tetramethylbutyl)-4-methoxyphenol

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,6-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-ethoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-n-propyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-(3'-n-hexyloxycarbonyl-2'-methyl-prop-2'-yl)-4-methoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-(3'-n-octyloxycarbonyl-2'-methyl-prop-2'-yl)-4-methoxyphenol

2,5-bis-(5'-iso-propyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-n-butyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-iso-butyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-n-pentyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-iso-pentyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-n-heptyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-cyclohexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-n-octyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-[5'-(2"-ethylhexyloxycarbonyl)-2'-methyl-pent-2'-yl]-4-methoxyphenol

2,5-bis-(5'-n-dodecyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-n-hexadecyloxycarbonyl-2'-pent-2'-yl)-4-methoxyphenol

2,5-bis-[5'-(2"-methoxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-methoxyphenol

2,5-bis-[5'-(2"-n-butyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-methoxyphenol

2,5-bis-[5'-(2"-cyclohexyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-methoxyphenol

2,5-bis-[5'-(2"-allyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-methoxyphenol

2,5-bis-[5'-(2"-benzyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-methoxyphenol

2,5-bis-[5'-(2"-phenoxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-methoxyphenol

2,5-bis-(5'-phenoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-benzyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-tetrahydrofurfuryloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-furfuryloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-[5'-(tetrahydropyran-4-yloxycarbonyl)-2'-methyl-pent-2'-yl]-4-methoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)-4-methoxyphenol and its sodium salt

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-ethoxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-n-propyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-n-butoxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-(3'-n-hexyloxycarbonyl-2'-methyl-prop-2'-yl)-4-ethoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-(3'-n-octyloxycarbonyl-2'-methyl-prop-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-iso-propyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-n-butyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-iso-butyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-n-pentyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-iso-pentyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-n-heptyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-cyclohexylcarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-n-octyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-[5'-(2"-ethylhexyloxycarbonyl)-2'-methyl-pent-2'-yl]-4-ethoxyphenol

2,5-bis-(5'-n-dodecyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-n-hexadecyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-[5'-(2"-methoxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-ethoxyphenol

2,5-bis-[5'-(2"-n-butyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-ethoxyphenol

2,5-bis-[5'-(2"-cyclohexyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-ethoxyphenol

2,5-bis-[5'-(2"-allyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-ethoxyphenol

2,5-bis-[5'-(2"-benzyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-ethoxyphenol

2,5-bis-[5'-(2"-phenoxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-ethoxyphenol

2,5-bis-(5'-phenoxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-benzyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-tetrahydrofurfuryloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-furfuryloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-[5'-(tetrahydropyran-4"-yloxycarbonyl)-2'-methyl-pent-2'-yl]-4-ethoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)-4-ethoxyphenol and its sodium salt

2,5-bis-(2'-methyl-6'-hydroxy-hex-2'-yl)-4-ethoxyphenol

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-ethoxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-n-propyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-(3'-n-hexyloxycarbonyl-2'-methyl-prop-2'-yl)-4-n-butoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-(3'-n-octyloxycarbonyl-2'-methyl-prop-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-iso-propyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-n-butyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-iso-butyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-n-pentyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-iso-pentyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-n-heptyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-cyclohexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-n-octyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-[5'-(2"-ethylhexyloxycarbonyl)-2'-methyl-pent-2'-yl]-4-n-butoxyphenol

2,5-bis-(5'-n-dodecyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-n-hexadecyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-[5'-(2"-methoxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-n-butoxyphenol

2,5-bis-[5'-(2"-n-butyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-n-butoxyphenol

2,5-bis-[5'-(2"-cyclohexyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-n-butoxyphenol

2,5-bis-[5'-(2"-allyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-n-butoxyphenol

2,5-bis-[5'-(2"-benzyloxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-n-butoxyphenol

2,5-bis-[5'-(2"-phenoxyethoxycarbonyl)-2'-methyl-pent-2'-yl]-4-n-butoxyphenol

2,5-bis-(5'-phenoxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-benzyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-tetrahydrofurfuryloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-furfuryloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-Bis-[5'-(tetrahydropyran-4"-yloxycarbonyl)-2'-methyl-pent-2'-yl]-4-n-butoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol

2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)-4-n-butoxyphenol and its sodium salt

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-n-hexyloxyphenol

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-cyclohexyloxyphenol

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-(2'-n-butoxyethoxy)-phenol

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-(2'-ethylhexyloxy)-phenol

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-n-dodecyloxyphenol

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-n-hexadecyloxyphenol

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-benzyloxyphenol

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-phenoxyphenol

2,5-bis-(5'-cyano-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-carbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-N-n-butylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-N-N-dimethylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-N-n-octylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-N,N-di-n-butylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-N-eicosylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-N-allylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-N-cyclohexylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-N-benzylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-N-phenylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5'-morpholinocarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2-(7'-methoxycarbonyl-2',2',4'-trimethyl-hept-4'-yl)-5-t-butyl-4-methoxyphenol

2-(1',7'-di-methoxycarbonyl-4'-methyl-hept-4'-yl)-4-methoxyphenol

2,5-bis-(2'-methyl-6'-hydroxy-hex-2'-yl)-4-methoxyphenol

2,5-bis-(2',6'-dimethyl-8'-hydroxy-oct-2'-yl)-4-methoxyphenol

2,5-bis-(8'-acetyloxy-2',6'-dimethyl-oct-2'-yl)-4-methoxyphenol

2,5-bis-(2',6'-dimethyl-8'-propionyloxy-oct-2'-yl)-4-methoxyphenol

2,5-bis-(8'-butyryloxy-2',6'-dimethyl-oct-2'-yl)-4-methoxyphenol

2,5-bis-(2',6'-dimethyl-8'-hexanoyloxy-oct-2'-yl)-4-methoxyphenol

2-(5'-diethylphosphono-5'-ethoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(5',5'-di-ethoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(2',6'-dimethyl-8'-eicosanoyloxy-oct-2'-yl)-4-methoxyphenol

2,5-bis-(8'-crotonyloxy-2',6'-dimethyl-oct-2'-yl)-4-methoxyphenol

2,5-bis-(8'-benzoyloxy-2',6'-dimethyl-oct-2'-yl)-4-methoxyphenol

2,5-bis-(2',6'-dimethyl-8'-phenacetyloxy-oct-2'-yl)-4-methoxyphenol

2,5-bis-(8'-cyclohexylcarbonyloxy-2',6'-dimethyl-oct-2'-yl)-4-methoxyphenol

2,5-bis-(8'-methoxy-2',6'-dimethyl-oct-2'-yl)-4-methoxyphenol

2,5-bis-(8'-butoxy-2',6'-dimethyl-oct-2'-yl)-4-methoxyphenol

2,5-bis-(8'-pentadecyloxy-2',6'-dimethyl-oct-2'-yl)-4-methoxyphenol

2 and 3-(8'-amino-2',6'-dimethyl-oct-2'-yl)-4-methoxyphenol

2,5-bis-(6'-amino-2'-methyl-hept-2'-yl)-4-methoxyphenol and its hydrochloride

2,5-bis-(6'-methylamino-2'-methyl-hept-2'-yl)-4-methoxyphenol

2,5-bis-(6'-N,N-dimethylamino-2'-methyl-hept-2'-yl)-4-methoxyphenol

2,5-bis-(6'-N-ethylamino-2'-methyl-hept-2'-yl)-4-methoxyphenol

2,5-bis-(6'-N,N-diethylamino-2'-methyl-hept-2'-yl)-4-methoxyphenol

2,5-bis-(6'-N-n-butylamino-2'-methyl-hept-2'-yl)-4-methoxyphenol

2,5-bis-(6'-N,N-di-n-butylamino-2'-methyl-hept-2'-yl)-4-methoxyphenol

2,5-bis-(2'-methyl-6'-morpholino-hept-2'-yl)-4-methoxyphenol

2 and 3-(6'-acetamido-2'-methyl-hept-2'-yl)-4-methoxyphenol

2,5-bis-(6'-acetamido-2'-methyl-hept-2'-yl)-4-methoxyphenol

2,5-bis-(6'-hexanamido-2'-methyl-hept-2'-yl)-4-methoxyphenol

2,5-bis-(12'-amino-2',13'-dimethyl-tetradec-2'-yl)-4-methoxyphenol

2,5-bis-(12'-amino-3',13'-dimethyl-tetradec-3'-yl)-4-methoxyphenol

2,5-bis-(12'-acetamido-2',13'-dimethyl-tetradec-2'-yl)-4-methoxyphenol

2,5-bis-(12'-acetamido-3',13'-dimethyl-tetradec-3'-yl)-4-methoxyphenol

2-(2'-methyl-4'-phosphono-but-2'-yl)-4-methoxyphenol and its sodium salts

2-(2'-methyl-4'-dimethylphosphono-but-2'-yl)-4-methoxyphenol

2-(4'-diethylphosphono-2'-methyl-but-2'-yl)-4-methoxyphenol

2-(4'-di-n-butylphosphono-2'-methyl-but-2'-yl)-4-methoxyphenol

5-t-butyl-2-(2'-methyl-4'-dimethylphosphono-but-2'-yl)-4-methoxyphenol

5-(1',1',3',3'-tetramethylbutyl)-2-(2'methyl-4'-di-methylphosphonobut-2'-yl)-4-methoxyphenol

2,5-bis-(2'-methyl-4'-di-methylphosphono-but-2'-yl)-4-methoxyphenol

2,5-bis-(2'-methyl-4'-di-ethylphosphono-but-2'-yl)-4-methoxyphenol

2,5-bis-(2'-methyl-4'-di-n-propylphosphono-but-2'-yl)-4-methoxyphenol

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-5-(2'-methyl-4'-diethylphosphono-but-2'-yl)-4-methoxyphenol

2,5-bis-(2'-methyl-4'-di-iso-propylphosphono-but-2'-yl)-4-methoxyphenol

2,5-bis-(2'-methyl-4'-di-n-butyl-phosphono-but-2'-yl)-4-methoxyphenol

2,5-bis-[2'-methyl-4'-(di-2"-ethylhexyl-phosphono)-but-2'-yl]-4-methoxyphenol

2,5-bis-(2'-methyl-4'-di-n-dodecylphosphono-but-2'-yl)-4-methoxyphenol

2,5-bis-[2'-methyl-4'-(2"-oxo-1",3",2"-dioxaphospholan-2"-yl)-but-2'-yl]-4-methoxyphenol

2,5-bis-[2'-methyl-4'-(4"-methyl-2"-oxo-1",3",2"-dioxaphospholan-2"-yl)-but-2'-yl]-4-methoxyphenol

2,5-bis-[4'-(ethyl-ethylphosphino)-2'-methyl-but-2'-yl]-4-methoxyphenol

2,5-bis-(5'-ethoxycarbonyl-5'-diethylphosphono-2'-methyl-pent-2'-yl)-4-methoxyphenol

2,5-bis-(2'-methyl-3'-sulpho-prop-2'-yl)-4-methoxyphenol

2-(2'-methyl-3'-sulphonamido-prop-2'-yl)-4-methoxyphenol

5-t-butyl-2-(2'-methyl-3'-sulphonamido-prop-2'-yl)-4-methoxyphenol

2-(2'-methyl-3'-N-methylsulphonamido-prop-2'-yl)-4-methoxyphenol

5-(1',1',3',3'-tetramethylbutyl)-2-(2'-methyl-3'-N-methylsulphonamido-prop-2'-yl)-4-methoxyphenol

2-(2'-methyl-3'-N,N-di-n-butylsulphonamido-prop-2'-yl)-4-methoxyphenol

2-(2'-methyl-3'-N-n-octylsulphonamido-prop-2'-yl)-4-methoxyphenol

5-t-butyl-2-(2'-methyl-3'-N-n-octylsulfonamido-prop-2'-yl)-4-methoxyphenol

2-(7'-cyano-2',6'-dimethyl-hept-2'-yl)-4-methoxyphenol

2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'yl)-1,4-dimethoxybenzene

2-methyl-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2-t-butyl-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-5-(1',1',3',3'-tetramethylbutyl)-1,4-dimethoxybenzene

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2,5-bis-(5'-ethoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2,5-bis-(5'-n-propyloxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2,5-bis-(5'-iso-propyloxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2,5-bis-(5'-n-butoxycarbonyl-2'-methyl-pent-2'yl)-1,4-dimethoxybenzene

2,5-bis-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'yl)-1,4-dimethoxybenzene

2,5-bis-(5'-(2"-ethylhexyloxycarbonyl)-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2,5-bis-(5'-n-butoxyethoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2,5-bis-(5'-tetrahydrofurfuryloxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2,5-bis-(4'-keto-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene

2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2-methyl-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2-t-butyl-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-5-(1',1',3',3'-tetramethylbutyl)-1,4-diethoxybenzene

2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2,5-bis-(5'-ethoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2,5-bis-(5'-n-propyloxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2,5-bis-(5'-iso-propyloxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2,5-bis-(5'-n-butoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2,5-bis-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2,5-bis-[5'-(2"-ethylhexyloxycarbonyl)-2'-methyl-pent-2'-yl]-1,4-diethoxybenzene

2,5-bis-(5'-n-butoxyethoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2,5-bis-(5'-tetrahydrofurfuryloxycarbonyl-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)-1,4-diethoxybenzene

1-ethoxy-4-methoxy-2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-benzene

4-ethoxy-1-methoxy-2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-benzene

2-t-butyl-1-ethoxy-4-methoxy-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-benzene

2-t-butyl-4-ethoxy-1-methoxy-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-benzene

1-ethoxy-4-methoxy-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2-(1',1',3',3'-tetramethylbutyl)-benzene

4-ethoxy-1-methoxy-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2-(1',1',3',3'-tetramethylbutyl)-benzene

1-ethoxy-4-methoxy-2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-benzene

1-ethoxy-4-methoxy-2,5-bis-(5'-ethoxycarbonyl-2'-methyl-pent-2'-yl)-benzene

1-ethoxy-4-methoxy-2,5-bis-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-benzene

1-ethoxy-4-methoxy-2,5-bis-(5'-n-butoxyethoxycarbonyl-2'-methyl-pent-2'-yl)-benzene

1-ethoxy-4-methoxy-2,5-bis-(5'-tetrahydrofurfuryl-oxycarbonyl-2'-methyl-pent-2'-yl)-benzene

1-ethoxy-4-methoxy-2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)-benzene

5-hydroxy-6-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2,2-dimethylcoumaran

5-hydroxy-6-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-2,2-dimethylcoumaran

6-hydroxy-7-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2,2-dimethylchroman

6-hydroxy-7-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-2,2-dimethylchroman

6-hydroxy-7-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2,2,4-trimethyl-chroman

6-hydroxy-7-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-2,2,4-trimethyl-chroman

6-hydroxy-7-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2,2-dimethyl-4-isopropyl-chroman

6-hydroxy-7-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-2,2-dimethyl-4-isopropyl-chroman

6-hydroxy-7-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2-methyl-2-(4',8',12'-trimethyl-tridec-1'-yl)-chroman

bis-[5-hydroxy-2-methoxy-4-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-phenyl]-methane

bis-[5-hydroxy-2-methoxy-4-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-phenyl]-methane

bis-[2-hydroxy-5-methoxy-3-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-phenyl]-methane

bis-2,2-[2-hydroxy-5-methoxy-4-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-phenyl]-propane

bis-2,2-[2-hydroxy-5-methoxy-4-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-phenyl]-propane

bis-[4-hydroxy-2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)phenyl]-oxide

6-hydroxy-2-[2,5-dihydroxy-4-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)phenyl]-7-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2,4,4-trimethylchroman

6,6'-dihydroxy-7,7'-bis-(5"-methoxycarbonyl-2"-methyl-pent-2"-yl-4,4,4',4'-tetramethyl-2,2'-spiro-bis-chroman

5-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-2-cumyl-4-methoxyphenol

bis-[5-(2'-hydroxy-5'-methoxy-phenyl)-5-methyl-hexanoic acid] ester of hexane 1,6-diol

N,N'-[5-(2'-hydroxy-5'-methoxy-phenyl)-5-methyl-hexanoic acid]amide of hexane-1,6-diamine.

Other non-limiting examples of compounds of formula I viz. those wherein R_(o) is a group of formula IVa or IVb, as hereinbefore defined, are those having the formula: ##STR18## wherein J is a residue having the formula: ##STR19## Non limiting examples of compounds of formula XIV (page 34) are ##STR20## The present invention also provides a process for the production of compounds of formula I comprising reacting, in the presence of an acidic catalyst, a compound of formula X ##STR21## wherein R₁ ' is hydrogen, a C₁₋₈ straight or branched chain alkyl group, or C₇ -C₉ aralkyl, and R_(o) and R_(oo) have their previous significance, or R₁ ' and R_(o) together may form a residue of formula V as hereinbefore defined, with an alkylating agent capable of introducing one or two residues of formula II, as hereinbefore defined, or one residue of formula IX as hereinbefore defined, into either one or two aromatic rings of the compound of formula X.

The alkylation step is conveniently carried out at a temperature ranging from 20° C. to 150° C., but preferably in the range 20° C. to 100° C. The acid catalyst may be a Bronsted or Lewis acid or active earth. Bronsted acids suitable for the purpose may be organic or inorganic or a partial salt thereof and may be an inorganic acid such as hydrochloric, sulphuric, perchloric and orthophosphoric acid; an alkyl, aryl or alkaryl substituted inorganic acid such as methane and ethane sulphonic acids, benzene sulphonic acid, p-toluene sulphonic acid and methane phosphonic acid; an organic acid such as dichloroacetic acid, trichloroacetic acid, and trifluoroacetic acids. Lewis acids suitable for alkylation include boron trifluoride, ferric chloride, aluminium chloride and stannic chloride. Active earths suitable for alkylation include Fulmont 237® and Fulcat 22®.

The above-described catalysts may be used alone or in conjunction with a solvent or solvent mixture. Suitable solvents include ether, water, methanol, acetic acid, benzene and nitromethane. The preferred catalysts are sulphuric acid containing methanol, p-toluene sulphonic acid and aluminium chloride in combination with nitromethane solvent.

More specifically, compounds of formua I wherein q is 0 or and p is 1 or 2 may be produced by reacting, in the presence of an acidic catalyst, 1 mole of a compound of formula X wherein R_(o) and R_(oo) each have their previous signficance viz. a compound having the formula X as hereinbefore defined wherein R_(o) and R_(oo) have their previous significance and R₁ ' is as hereinbefore defined with from 0.1 to at least 2.0 moles of an alkylating agent capable of introducing the residue II into at least one aromatic ring of the compound of formula X.

Compounds of formula I wherein p is 1 and q is 1 may be produced by reacting, in the presence of an acidic catalyst, 1 mole of a compound of formula XI: ##STR22## wherein p is 1, R is a residue of formula II and R_(o) and R_(oo) have their previous significance, with at least 1.0 mole of an alkylating agent capable of introducing the residue II or IX into the ring of the compound of formula XI.

Compounds of formula IC ##STR23## where A is a carbon residue containing 4 to 20 carbon atoms which form a substituted chroman or coumaran system, and R and R_(oo) are as previously defined, may be produced by reacting in the presence of an acid catalyst, 1 mole of a compound of formula (XA) ##STR24## where R and R_(oo) are as previously defined, with at least 1 mole of an alkylating agent capable of introducing the residue A into the ring of the compound of formula (XA).

Alkylating agents which are suitable for this purpose have two reactive centres, and may be dienes, diols, hydroxy olefins, or halo olefins, such as isoprene, 2-methyl-penta-2,4-diene, 2-methylhexa-2,4-diene, 2,5-dimethyl-hexa-2,4-diene, methallyl alcohol, methallyl chloride, prenyl alcohol, phytol, 2-methyl-pentan-2,4-diol, 2,5-dimethyl-hexan-2,5-diol.

Compounds of formula Id ##STR25## where R_(x) and R_(y) are the same or different and are H or C₁ -C₄ alkyl, and R, R_(o) and R_(oo) are as previously defined, may be prepared by reacting in the presence of an acid catalyst, 1 mole of a compound of formula XIA ##STR26## where R, R_(o) and R_(oo) are as previously defined, with up to 0.5 moles of an aldehyde or ketone having 1-9 carbon atoms.

Compounds of formula Ie ##STR27## where R and R_(oo) are as previously defined, may be prepared by reacting in the presence of an acid catalyst, 1 mole of a compound of formula XA with at least 1.5 moles of acetone or with up to 0.5 moles of phorone.

Compounds of formula If ##STR28## where R and R_(oo) are as previously defined, may be prepared by reacting, in the presence of an acid, 1 mole of a compound of formula XA with at least 1 mole of acetone or with up to 0.5 moles of mesityl oxide.

In a further process, the compounds of formula I wherein R₁ is C₁ -C₈ alkyl, C₇ -C₉ aralkyl or a residue of formula II or III, one of R_(o) and R_(oo) is hydrogen and the other R_(o) or R_(oo) is a C₁ -C₂₀ straight- or branched alkyl optionally interrupted by 1 to 5 oxygen atoms, a C₃ -C₁₂ cycloalkyl group, a C₆ -C₁₀ aryl group or a C₇ -C₁₃ aralkyl group and R has its previous significance, may be produced by reacting a compound of formula XII ##STR29## in the presence of a quinone, preferably the corresponding quinone analogue of formula XIII: ##STR30## wherein in formula XII and XIII R₁ is C₁₋₈ alkyl, C₇₋₉ aralkyl or a residue of formula II or III and R, p and q have their previous significance, with a compound having the formula R_(o) --OH or R_(oo) --OH wherein R_(o) and R_(oo) are the same or different and are a C₁ -C₂₀ straight or branched alkyl group optionally interrupted by 1 to 5 oxygen atoms, a C₃ -C₁₂ cycloalkyl group, a C₆ -C₁₀ aryl group or a C₇ -C₁₃ aralkyl group in an acidic medium. Further details of this process as described in GB Patent No. 1557237.

In a further process according to the invention, compounds of formula I wherein one of R_(o) and R_(oo) is hydrogen are produced by reacting the quinone analogues of formula XIII with a compound of formula (R_(o) O)₃ P or (R_(oo) O)₃ P, wherein R_(o) and R_(oo) are the same or different and are a C₁ -C₂₀ straight or branched alkyl group optionally interrupted by 1 to 5 oxygen atoms, a C₃ -C₁₂ cycloalkyl group, a C₆ -C₁₀ aryl group atoms or a C₇ -C₁₃ aralkyl group and then hydrolysing the resulting phosphate using the method described by F. Ramirez et al. J. Am. Chem. Soc. 81, 4338, 1959.

In a still further process, compounds of formula I wherein each of R_(o) and R_(oo) is other than hydrogen may be produced by reacting a compound of formula I wherein R_(o) and R_(oo) are each hydrogen, or one is hydrogen, with a compound R_(o) --OH (or R_(oo) --OH) in an acidic medium or with a compound R_(o) --X or (R_(oo) --X) or (R_(o))₂ SO₄ or (R_(oo))₂ SO₄, in an alkaline medium, wherein R_(o) and R_(oo) are the same or different and are a C₁ -C₂₀ straight or branched alkyl group optionally interrupted by 1 to 5 oxygen atoms, a C₃ -C₁₂ cycloalkyl group, a C₆ -C₁₀ aryl group or a C₇ -C₁₃ aralkyl group and X is halogen.

Compounds of formula XII wherein R₁ is C₇ -C₉ aralkyl are new compounds. Compounds of formula XII may be prepared by reacting, in the presence of an acid catalyst, a hydroquinone of formula X (R_(o) and R_(oo) both being hydrogen and R₁ ' is hydrogen or C₁ -C₈ alkyl or C₇ -C₉ aralkyl) with a functional alkylating agent capable of introducing p moles of a group R, as hereinbefore defined. Examples of suitable functional alkylating agents are set out hereinafter.

Compounds of formula XII which contain a residue of formula III are also novel and have the formula XIV ##STR31## in which R, M and p have their previous significance. Compounds of formula XIV are active as stabilisers for magenta couplers.

Compounds of formula XIV may be produced by methods well known per se e.g. by condensing 2 moles of a compound of formula XII where q=0 with an agent capable of introducing the linkage --M--.

Compounds XIII are also new compounds and may be produced by oxidising the compounds of formula XII. Examples of suitable oxidising agents are salts of an element capable of abstracting electrons and possessing a suitable redox potential; a hypohalite; a perhalate; nitric acid; an oxide of nitrogen; chromium trioxide, a chromate, Jones' reagent, an organic oxidizing agent; oxygen or air, optionally catalysed by metal salts.

The preparation of compounds of formula I wherein R_(o) is a group of formula IVa or IVb, as hereinbefore defined, may be effected by reacting either 2 or 3 moles of a compound of formula XII A: ##STR32## wherein R, R₁ ", p and q have their previous significance, in the presence of a base, with a corresponding di- or tri-halide Hal-B(Hal)_(m), epichlorohydrin, epibromohydrin, or a diglycidyl ether compound ##STR33## respectively; or by reacting a compound of formula XIIA, in the presence of a base, with a halide ##STR34## wherein m, r, B, R, R₁₆ and D have their previous significance and Hal represents chlorine and, especially, bromine.

The compounds of formula XII A may be prepared in the manner previously described for the production of compounds of formula XII, by reacting, in the presence of an acid catalyst, a compound of formula X wherein R_(o) and R_(oo) are each hydrogen, with a functional alkylating agent capable of introducing one or two residues of formula II as hereinbefore defined.

Non limiting examples of compound of formula X include:

hydroquinone-monomethyl ether

hydroquinone-monoethyl ether

hydroquinone-mono-n-propyl ether

hydroquinone-mono-iso-propyl ether

hydroquinone-mono-n-butyl ether

hydroquinone-mono-sec-butyl ether

hydroquinone-mono-n-pentyl ether

hydroquinone-mono-n-hexyl ether

hydroquinone-mono-n-octyl ether

hydroquinone-mono-2-ethylhexyl ether

hydroquinone-mono-dodecyl ether

hydroquinone-mono-hexadecyl ether

hydroquinone-mono-cyclohexyl ether

hydroquinone-mono-n-butoxyethyl ether

hydroquinone-mono-benzyl ether

hydroquinone-mono-phenyl ether

2-methyl-4-methoxyphenol

2-ethyl-4-methoxyphenol

2-iso-propyl-4-methoxyphenol

2-t-butyl-4-methoxyphenol

2-(1',1',3',3'-tetramethylbutyl)-4-methoxyphenol

1,4-dimethoxybenzene

2-methyl-1,4-dimethoxybenzene

2-t-butyl-1,4-dimethoxybenzene

1,4-diethoxybenzene

2-methyl-1,4-diethoxybenzene

2-t-butyl-1,4-diethoxybenzene

1,4-di-n-propoxybenzene 1,4-di-n-butoxybenzene

2-t-butyl-1-ethoxy-4-methoxybenzene

Functional alkylating agents capable of introducing a residue a formula II which are reacted with the hydroquinone contain a reactive centre, for example, an olefinic or hydroxy group which is eliminated, transformed or rearranged during the course of the alkylation reaction.

Examples of functional olefins suitable for the functional alkylation of compounds of formula X, XA and XI are:

5-methylhex-5-enoic acid

methyl 5-methylhex-5-enoate

ethyl 5-methylhex-5-enoate

n-propyl 5-methylhex-5-enoate

iso-propyl 5-methylhex-5-enoate

n-butyl 5-methylhex-5-enoate

iso-butyl 5-methylhex-5-enoate

sec-butyl 5-methylhex-5-enoate n-pentyl 5-methylhex-5-enoate

iso-pentyl 5-methylhex-5-enoate

sec-pentyl 5-methylhex-5-enoate

n-hexyl 5-methylhex-5-enoate

cyclohexyl 5-methylhex-5-enoate

2-ethylhexyl 5-methylhex-5-enoate

n-octyl 5-methylhex-5-enoate

n-dodecyl 5-methylhex-5-enoate

n-hexadecyl 5-methylhex-5-enoate

methyl 5,7,7-trimethyl-oct-4-enoate

1,7-di-methoxycarbonyl-4-methyl-hept-3-ene

4-carbomethoxy-1-methylcyclohex-1-ene

4-acetyl-1-methylcyclohex-1-ene

4,5-bis-carbomethoxy-1-methylcyclohex-1-ene

dimethylprenylphosphonate

diethylprenylphosphonate

dipropylprenylphosphonate

di-isopropylprenylphosphonate

di-n-butylprenylphosphonate

di-n-octylprenylphosphonate

citronellol

citronellyl acetate

citronellyl methyl ether

citronellyl butyl ether

2-amino-6-methyl-hept-5-ene

2-amino-6-methyl-hept-6-ene

diethyl 2-ethoxycarbonyl-5-methyl-hex-4-ene-2-phosphonate

ethyl 2-ethoxycarbonyl-5-methyl-hex-4-enoate

citronellylnitrile

2-acetamido-6-methyl-hept-5-ene

2-acetamido-6-methyl-hept-6-ene

2-methyl-2-propene-1-sulphonic acid

2-methyl-2-propene-1-sulphonic acid amide

N-n-butyl-2-propene-1-sulphonic acid amide

N,N-di-n-butyl-2-propene-sulfphonic acid amide

N-n-octyl-2-propene-1-sulfphonic acid amide

Examples of functional hydroxy compounds suitable for the functional alkylation of compounds of formula X, XA and XI are

2-amino-6-hydroxy-6-methylheptane

2-acetamido-6-hydroxy-6-methylheptane

11-amino-2,2,12-trimethyl-tridecan-1-ol

as well as members selected from 11-amino-undecanols of the formula: ##STR35## wherein Y₁ and Y₃, independently, are --H or C₁ -C₈ alkyl; Y₂ and Y₄, independently, are C₁ -C₈ alkyl; and Y₅ and Y₆, independently, are --H or C₁ -C₄ alkyl.

These 11-amino-undecanols are described in more detail, together with their method of manufacture in German Offenlegungsschrift No. 2831299.

Examples of olefins suitable of the alkylation of compounds of formula XI wherein p is 1, R₁, R_(o) and R_(oo) have their previous significance and R is a residue of formula II are isobutylene, diisobutylene and α-methyl styrene. Examples of alcohols suitable for the alkylation of compounds of formula XI wherein p is 1 and R₁, R_(o) and R_(oo) have their previous significance are t-butanol, 1,1,3,3-tetramethyl-butan-1-ol and cumyl alcohol.

Any functional derivative of a compound of formula I may be converted to a different functional derivative. For example when Q is the acid group --CO₂ H it may be esterified with an alcohol R₄ OH to give the corresponding ester --CO₂ R₄, or when Q is the ester group --CO₂ R₄ it may be transesterified to give a different R₄ group, or alternatively the ester group --CO₂ R₄ may be converted to an amide --CON(R₄)(R₅) by treatment with NH(R₄)(R₅), wherein R₄ and R₅ have their previous significance.

The compounds of formula I provide a valuable means of introducing a wide variety of functional residues for optimal photographic effect. For example, the polarity of and/or ballast in hydroquinone ethers of formula I are able to be regulated, and hence provide an effective control of solubility, compatibility, mobility/immobility for photographic systems. Such qualities make the compounds of formula I valuable intermediates for the preparation of more complex photographically useful compounds and render them useful as photographic stabilisers. A particularly advantageous property exhibited by the compounds of formula I, when used as photographic stabilisers, is that they do not have a deleterious effect on the dye yield, in contrast with previously-known substituted hydroquinones which reduce dye yield.

The compounds of the formula (I) as well as colour couplers can be incorporated in a known manner in photographic layers, for example in silver halide emulsions containing gelatin and/or other binders. For example, they can be used in silver bromide, silver chloride or silver iodide emulsions or in those emulsions which contain a mixture of silver halides, such as silver bromide/iodide or silver chloride/bromide emulsions.

The emulsions can be chemically sensitised and they can also contain further known organic stabilisers, such as hindered amines, phenolic compounds such as hindered phenols, alkoxyphenols, aryloxyphenols, hydroxycoumarans, hydroxychromans or dihydroxyspirochromans, or hydroquinones and especially hydroquinones of formula XII, whereby synergistic effects may be achieved, and UV absorbers, optical brightening agents and photographically active compounds such as antifogging agents or compounds which release a photographically active chemical such as DIR compounds, as well as customary plasticisers, for example glycerine. The emulsions can also be hardened with the hardeners customary for gelatin, furthermore the emulsions can contain customary coating assistants.

The emulsions can be applied to layer supports customary for photographic recording material. Optionally, a mixture of several colloids can be used to disperse the silver halides. The emulsions can also contain couplers, either alone or as a mixture, producing dyes during development, e.g. yellow, magenta, cyan or black dyes.

The customary developer baths can be employed for developing the recording material for colour photography. These baths as a rule contain a developer substance of the p-phenylenediamine type, a development retarder, such as potassium bromide, an antioxidant, such as sodium sulfite, a salt of sulfurous acid and/or hydroxylamine, and a base for example an alkali metal hydroxide or alkali metal carbonate. Furthermore, the developer baths can contain a conventional antifogging agent, complexing agents, wetting agents, optical brightening agents and others.

Corresponding application possibilities are described, for example, in U.S. Pat. Nos. 2,304,939, 2,304,940, 2,322,027, 2,284,879, 2,801,170, 2,801,171, 2,749,360 and 2,825,382.

The following examples further illustrate the present invention. Parts and percentages shown therein are by weight.

EXAMPLE 1

(a) 100 parts of 98% sulphuric acid are added to 32 parts of methanol keeping the temperature below 10° C. To this solution is then added 35.5 parts of methyl 5-methyl-hex-5-enoate followed by 12.4 parts of hydroquinone monomethyl ether. After stirring for 24 hours at room temperature the reaction mixture is poured into water, and the oil which separated extracted with ether. The ether extract after washing with 2N sodium hydroxide solution and then water is evaporated. Dilution of this oil with 40°-60° petroleum ether containing a little ether gives 2,5-bis-(5'-methoxycarbonyl-2'-methylpent-2'-yl)-4-methoxyphenol m.p. 82°-4° C. with the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             67.99   9.16                                                 Calculated for C.sub.23 H.sub.36 O.sub.6                                                         67.62   8.88                                                 ______________________________________                                    

(b) The sodium hydroxide washings from the above ether extract are heated on a steam-bath for 2 hours and then acidified. The solid obtained is filtered off, washed with water, and then crystallised from glacial acetic acid-water to give 2,5-bis-(5'-carboxy-2'-methylpent-2'yl)-4-methoxyphenol with m.p. 177°-9° C. and the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             65.80   8.31                                                 Calculated for C.sub.21 H.sub.32 O.sub.6                                                         66.29   8.48                                                 ______________________________________                                    

EXAMPLE 2a

110 Parts of hydroquinone, 284 parts of methyl 5-methylhex-5-enoate, and 10 parts of p-toluene sulphonic acid are heated on a steam-bath for 24 hours. The cooled reaction mixture partially solidified and after trituration with ether, yields after filtration, 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-hydroquinone, m.p. 150°-3° C. After crystallisation from ethanol/water. The product has m.p. 160°-2° C. with the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             67.05   8.96                                                 Calculated for C.sub.22 H.sub.34 O.sub.6                                                         66.98   8.69                                                 ______________________________________                                    

EXAMPLE 2b

44 Parts of 2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)hydroquinone are added in portions to 375 parts of 10-14% w/v aqueous sodium hypochlorite solution with vigorous stirring, the temperature being maintained between 25°-30° C. with a cold water bath. The mixture is stirred at room temperature for 1 hour, diluted with 300 parts of water, and acidified with concentrated hydrochloric acid to give, after filtration, 2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)-1,4-benzoquinone. After crystallisation from methanol the product has a m.p. of 204°-6° C. From methyl alcohol and 2,5-bis-(5'-carboxy-2'-methylpent-2'-yl)-1,4-benzoquinone using hydrogen chloride as a catalyst is prepared 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-benzoquinone as a bright yellow crystalline solid m.p. 85°-7° C. with the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             67.56   8.20                                                 Calculated for C.sub.22 H.sub.32 O.sub.6                                                         67.32   8.22                                                 ______________________________________                                    

EXAMPLE 2c

3.9 Parts of 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-hydroquinone (Example 2a), 0.4 parts of 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-benzoquinone (Example 2b), 1.0 parts of p-toluene sulphonic acid, and 50 parts of methanol are refluxed for 48 hours. After removing the excess methanol under reduced pressure, the residue is taken up in ether, and the ether extract washed first with sodium carbonate solution and then water. Evaporation of the ether gives a solid residue which is shown by GLC analysis to have the following percentage composition by weight.

    ______________________________________                                         Compound                    %                                                  ______________________________________                                         2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-                                                         21.3                                               1,4-dimethoxybenzene                                                           2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-                                                         67.0                                               4-methoxyphenol                                                                2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-                                                         11.7                                               hydroquinone                                                                   ______________________________________                                    

Crystallisation of the above solid mixture from 40°-60° petroleumether gives the 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol m.p. 81°-3° C. identical with that obtained in Example 1.

EXAMPLE 3

3.5 Parts of 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol, 100 parts of n-hexanol, and 0.5 parts of p-toluene sulphonic acid are heated on a steam-bath for 48 hours. At the end of the heating period the excess hexanol is removed by rota-evaporator under reduced pressure, and the residual oil taken up in ether. The ether solution is washed first with sodium bicarbonate solution then with water, and evaporated. Short-path distillation of the residue gives 2,5-bis-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol as a pale yellow viscous oil with the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             72.33   10.45                                                Calculated for C.sub.33 H.sub.56 O.sub.6                                                         72.22   10.29                                                ______________________________________                                    

EXAMPLE 4

2.3 Parts of 2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)-4-methoxyphenol, 50 parts of tetrahydrofurfuryl alcohol and 0.2 parts of p-toluene sulphonic acid are heated on a steam-bath for 18 hours. The excess alcohol is then removed by rota-evaporator under reduced pressure, and the residual oil taken up in ether. The ether solution after being washed with sodium bicarbonate solution and water is then evaporated to leave 2,5-bis-(5'-tetrahydrofurfuryloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol as an oil with the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             67.97   9.09                                                 Calculated for C.sub.31 H.sub.48 O.sub.8                                                         67.86   8.82                                                 ______________________________________                                    

EXAMPLE 5

2,5-Bis-(5'-n-butoxyethoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol is prepared by the procedure described in Example 4 using n-butoxyethanol in place of the tetrahydrofurfuryl alcohol. This ester obtained as an oil has the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             68.33   9.67                                                 Calculated for C.sub.33 H.sub.56 O.sub.8                                                         68.24   9.72                                                 ______________________________________                                    

EXAMPLE 6

(a) Example 1 is repeated using 13.8 parts of hydroquinone mono-ethyl ether in place of the hydroquinone mono-methyl ether. In this way there is obtained, 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol as an oil, b₀.7 210° C. (short-path distillation). (b₀.7 =boiling point at 0,7 millibar).

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             68.45   9.31                                                 Calculated for C.sub.24 H.sub.38 O.sub.6                                                         68.22   9.06                                                 ______________________________________                                    

(b) In a similar manner to Example 1b there is obtained 2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)-4-ethoxyphenol with m.p. 169°-71° C.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             67.13   8.72                                                 Calculated for C.sub.22 H.sub.34 O.sub.6                                                         66.98   8.69                                                 ______________________________________                                    

EXAMPLE 7

The acid of Example 6b is esterified with ethanol by the procedure of Example 4 to give 2,5-bis-(5'-ethoxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol and has m.p. 52°-4° C. from 40°-60° petroleumether

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             69.91   9.44                                                 Calculated for C.sub.26 H.sub.42 O.sub.6                                                         69.30   9.36                                                 ______________________________________                                    

EXAMPLE 8

In a similar manner to Example 4 the acid of Example 6b is reacted with n-hexanol to give 2,5-bis-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol as an oil after a short-path distillation at 0.7 mb.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             72.61   10.39                                                Calculated for C.sub.34 H.sub.58 O.sub.6                                                         72.56   10.39                                                ______________________________________                                    

EXAMPLE 9

In a similar manner to Example 1a and 1b using 16.6 parts of hydroquinone mono-n-butyl ether in place of hydroquinone monomethyl ether there is obtained:

(a) 2,5-Bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol b₀.9 238°-40° C.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             69.33   9.52                                                 Calculated for C.sub.26 H.sub.42 O.sub.6                                                         69.30   9.39                                                 ______________________________________                                    

and

(b) 2,5-bis-(5'-carboxy-2'-methyl-pent-2'-yl)-4-n-butoxyphenol m.p. 141°-3° C. from glacial acetic acid/water.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             68.12   9.19                                                 Calculated for C.sub.24 H.sub.38 O.sub.6                                                         68.22   9.06                                                 ______________________________________                                    

(c) The acid from 9b is esterified with isopropanol by the procedure of Example 4 to give 2,5-bis-(5'-isopropyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol with m.p. 62°-4° from 40°-60° petroleum-ether at -20° C.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             71.37   10.00                                                Calculated for C.sub.30 H.sub.50 O.sub.6                                                         71.11    9.95                                                ______________________________________                                    

and

(d) The acid from 9b is esterified with n-hexanol in the manner described in Example 4 to give 2,5-bis-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-n-butoxyphenol as an oil after a short-path distillation at 0.3 mb

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             73.09   10.51                                                Calculated for C.sub.36 H.sub.62 O.sub.6                                                         73.18   10.58                                                ______________________________________                                    

EXAMPLE 10

62.0 Parts of hydroquinone monomethyl ether, 28.4 parts of methyl 5-methyl-hex-4-enoate, and 2.0 parts of p-toluene sulphonic acid are heated on a steam-bath for 5 days. The reaction mixture is then diluted with ether and washed first with 2N sodium hyroxide solution and then water. After evaporation of the ether, the residue is distilled to give 2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol with b₀.1 154° C. and the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             67.92   8.56                                                 Calculated for C.sub.15 H.sub.22 O.sub.4                                                         67.65   8.33                                                 ______________________________________                                    

Acidification of the above alkaline washings gives an oil which after isolation with ether is distilled to give 3-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol b₀.4 172° C.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             67.47   8.32                                                 Calculated for C.sub.15 H.sub.22 O.sub.4                                                         67.65   8.33                                                 ______________________________________                                    

EXAMPLE 11

To 6.8 parts of aluminium chloride dissolved in 25 parts of nitromethane is added 13.8 parts of hydroquinone dimethyl ether and 7.1 parts of methyl 5-methyl-hex-5-enoate dissolved in 25 parts nitromethane dropwise at room temperature. The reaction mixture is then stored at room temperature for 2 days before being poured into water. The organic phase is ether extracted, and the ether extract is washed in turn with water, 2N sodium hydroxide solution, water, and then evaporated. Distillation of the residue gives 2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene with b₀.4 150° C. and the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             68.66   8.66                                                 Calculated for C.sub.16 H.sub.24 O.sub.4                                                         68.55   8.63                                                 ______________________________________                                    

EXAMPLE 12

The procedure described in Example 10 is repeated using twice the quantities of aluminium chloride and methyl 5-methyl-hex-5-enoate and gives bis-2,5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-1,4-dimethoxybenzene m.p. 81°-3° C. after crystallisation from 40°-60° petroleum ether

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             68.48   9.12                                                 Calculated for C.sub.24 H.sub.38 O.sub.6                                                         68.22   9.06                                                 ______________________________________                                    

EXAMPLE 13

2.5 Parts of 2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-hydroquinone, 1.5 parts of 2,5-dimethylhexa-2,4-diene, and 0.1 parts of p-toluene sulphonic acid are heated on a steam-bath for 3 days. The reaction after dilution with ether is washed first with 2N sodium hydroxide, followed by water, and the ether evaporated. Short path distillation of the residue at 0.3 mb gives 1.7 parts of lower boilers with the oven temperature at 175°, and then 6-hydroxy-7-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2,2-dimethyl-4-isopropylchroman with the oven temperature at 250°.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             72.15   9.56                                                 Calculated for C.sub.22 H.sub.34 O.sub.4                                                         72.89   9.45                                                 ______________________________________                                    

EXAMPLE 14

24.8 parts of p-methoxyphenol, 15.1 parts of citronellyl nitrile and 2.0 parts of p-toluene sulphonic acid are heated on a steam-bath for 3 days. The reaction mixture is then diluted with ether and the ether solution washed with sodium bicarbonate solution and water. After evaporation of the ether, the residue is distilled to give a mixture of 2- and 3-(7'-cyano-2',6'-dimethyl-hept-2'-yl)-4-methoxyphenol b₀.3 178°-86° C.

    ______________________________________                                                      Carbon Hydrogen  Nitrogen                                         ______________________________________                                         Found          74.14    9.15      5.09                                         Calculated for C.sub.17 H.sub.25 NO.sub.2                                                     73.91    9.39      5.18                                         ______________________________________                                    

EXAMPLE 15

To a stirred suspension of 4.0 parts of lithium aluminium hydride in 100 parts of ether, there is added 5.5 parts of 2- and 3-(7'-cyano-2',6'-dimethyl-hept-2'-yl)-4-methoxyphenol from Example 14, in 50 parts of ether, dropwise over 30 minutes. On completing the addition, stirring is continued for a further 2 hours before ethyl acetate is added to destroy unreacted lithium aluminium hydride. To the reaction mixture is then added 100 parts of 10N sodium hydroxide solution and the aqueous phase separated off from the ether solution. After washing the ether solution with water, the ether is evaporated and the residue distilled to give a mixture of 2- and 3-(8'-amino-2',6'-dimethyl-oct-2'-yl)-4-methoxyphenol b₀.7 182°-5° C. as a colourless oil with the following percentage composition by weight.

    ______________________________________                                                      Carbon Hydrogen  Nitrogen                                         ______________________________________                                         Found          72.91    10.46     4.80                                         Calculated for C.sub.17 H.sub.29 NO.sub.2                                                     73.07    10.46     5.01                                         ______________________________________                                    

EXAMPLE 16

By the same procedure of Example 15, 9.2 parts of 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-ethoxyphenol is reduced with 4.0 parts of lithium aluminium hydride and gives 2,5-bis-(6'-hydroxy-2'-methyl-hex-2'-yl)-4-ethoxyphenol b₀.7 230° C. as a pale yellow oil with the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             72.16   10.69                                                Calculated for C.sub.22 H.sub.38 O.sub.4                                                         72.09   10.45                                                ______________________________________                                    

EXAMPLE 17

62 parts of p-methoxyphenol, 17.8 parts of dimethylprenyl phosphonate, and 5.0 parts of Fulcat 22® are stirred at 125°-30° C. for 24 hours. The reaction mixture, after cooling, is diluted with methanol and filtered free of the catalyst. After removing the methanol under reduced pressure on a rota-evaporator, the residual oil is distilled to remove unreacted p-methoxyphenol (b₀.7 115° C.). The residual oil is then chromatographed on a column prepared from 200 parts of silica made up in 40°-60° petroleum ether. Elution with petroleum and then with petroleum containing increasing amounts of ether gives 2-(2'-methyl-4'-dimethylphosphonobut-2'-yl)-4-methoxyphenol as white prisms m.p. 97°-9° C. from ether.

    ______________________________________                                                      Carbon                                                                               Hydrogen  Phosphorous                                       ______________________________________                                         Found          56.00   7.52      10.13                                         Calculated for C.sub.14 H.sub.23 O.sub.5 P                                                    55.62   7.67      10.25                                         ______________________________________                                    

EXAMPLE 18

12.4 parts of p-methoxyphenol and 9.4 parts of N-acetylheptaminol are reacted together using the procedure of Example 1 and gives, as product, a mixture of 2- and 3-(6'-acetamido-2'-methylhept-2'-yl)-4-methoxyphenol. The 2-isomer is obtained as a white crystalline solid m.p. 118°-20° C. after crystallisation from ether containing a little acetone.

    ______________________________________                                                      Carbon Hydrogen  Nitrogen                                         ______________________________________                                         Found          69.65    9.62      4.87                                         Calculated for C.sub.17 H.sub.27 NO.sub.3                                                     69.59    9.28      4.77                                         ______________________________________                                    

EXAMPLE 19

8.2 parts of 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol and 50 parts of n-octylamine are refluxed together for 20 hours. After removing the excess octylamine under reduced pressure, the residue is diluted with 40°-60° petroleum-ether containing a little ether and gives 2,5-bis-(5'-N-n-octylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol m.p. 86°-90° C.

    ______________________________________                                                       Carbon Hydrogen  Nitrogen                                        ______________________________________                                         Found           73.54    11.88     4.81                                        Calculated for C.sub.37 H.sub.66 N.sub.2 O.sub.4                                               73.71    11.03     4.65                                        ______________________________________                                    

EXAMPLE 20

5.0 parts of 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol and 20 parts of di-n-butylamine are sealed into a glass tube and heated at 200° C. for 48 hours. The excess dibutylamine is removed under reduced pressure and gives 2,5-bis-(5'-N,N-di-n-butylcarbamoyl-2'-methyl-pent-2'-yl)-4-methoxyphenol as a pale yellow viscous syrup with the following percentage composition by weight:

    ______________________________________                                                       Carbon Hydrogen Nitrogen                                         ______________________________________                                         Found           73.80    10.91    4.38                                         Calculated for C.sub.37 H.sub.66 N.sub.2 O.sub.4                                               73.71    11.03    4.65                                         ______________________________________                                    

EXAMPLE 21

24.8 parts of p-methoxyphenol, 13.8 parts of 4-acetyl-1-methylcyclohex-1-ene and 2.0 parts of p-toluene sulphonic acid are heated on a steam-bath for 3 days and the reaction mixture then diluted with ether. After washing the ether extract with 2N sodium hydroxide, and water, the ether is evaporated and the residue distilled to give a mixture of cis- and trans-2-(4'-acetyl-1'-methylcyclohex-1'-yl)-4-methoxyphenol b₀.3 200°-20° C.

    ______________________________________                                                         Carbon    Hydrogen                                             ______________________________________                                         Found             75.81       8.96                                             Calculated for C.sub.16 H.sub.22 O.sub.3                                                         73.25       8.45                                             ______________________________________                                    

EXAMPLE 22

Example 21 is repeated except that 21.2 parts of 4,5-bis-carbomethoxy-1-methylcyclohex-1-ene is used in place of the 4-acetyl-1-methyl-cyclohex-1-ene. Distillation gives 2- and 3-(3',4'-bis-methoxycarbonyl-1'-methyl-cyclohex-1'-yl)-4-methoxyphenol b₀.3 218°-24° C.

    ______________________________________                                                         Carbon    Hydrogen                                             ______________________________________                                         Found             64.23       7.44                                             Calculated for C.sub.18 H.sub.24 O.sub.6                                                         64.27       7.19                                             ______________________________________                                    

EXAMPLE 23

10.0 parts of 2,5-bis-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol, 50 parts of cetyl alcohol and 1.0 parts of p-toluene sulphonic acid are heated on a steam-bath for 3 days. At the end of the heating period most of the excess cetyl alcohol is removed by rota-evaporator under reduced pressure, and the residual oil taken up in ether. The ether solution is washed first with sodium bicarbonate solution then with water and evaporated. The residual oil is finally stripped down on a rotary-still at 0.7 mb at a temperature of 230° C., and gives 2,5-bis-(5'-hexadecycloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol as a viscous oil with the following percentage composition by weight.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             77.15   11.90                                                Calculated for C.sub.53 H.sub.96 O.sub.6                                                         76.81   11.59                                                ______________________________________                                    

EXAMPLE 24

Example 17 is repeated except that 30.6 parts of diethyl 2-ethoxycarbonyl-5-methyl-hex-4-ene-2-phosphonate are used in place of dimethyl prenyl phosphonate, and there is obtained 2- and 3-(5'-ethoxycarbonyl-5'-diethylphosphono-2'-methyl-pent-2'-yl)-4-methoxyphenol as a viscous oil.

    ______________________________________                                                      Carbon                                                                               Hydrogen  Phosphorous                                       ______________________________________                                         Found          58.51   8.12      6.95                                          Calculated for C.sub.21 H.sub.35 O.sub.7 P                                                    58.59   8.19      7.19                                          ______________________________________                                    

EXAMPLE 25

5.0 parts of 2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-hydroquinone, 1.9 parts 1,4-bis-(2'-hydroxy-prop-2'-yl)-benzene, and 0.2 parts of p-toluene sulphonic acid in 25 parts of benzene are refluxed for 24 hours. The reaction mixture after cooling is diluted with ether, and the ether solution washed with 2N sodium hydroxide solution, and water. Evaporation of the ether gives a solid residue which, after crystallisation from benzene, gives 1,4-bis-{2-[2,5-dihydroxy-4-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-phenyl]-prop-2-yl}-benzene m.p. 198°-201° C.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             72.68   8.39                                                 Calculated for C.sub.40 H.sub.54 O.sub.8                                                         72.48   8.21                                                 ______________________________________                                    

EXAMPLE 26

6.9 parts of hydroquinone dimethyl ether, 6.2 parts of N-N-octyl-2-propene-1-sulphonic acid amide and 13.4 parts of anhydrous aluminium chloride in 50 parts of nitromethane are stored for 3 days at room temperature. The reaction mixture is then poured into water and the organic material extracted with ether. After washing the ether extract with water and evaporating off solvents, the residue is chromatographed on silica and gives 2-(2'-methyl-3'-N-n-octylsulphonamido-prop-2'-yl)-4-methoxyphenol as a viscous oil.

    ______________________________________                                                       Carbon Hydrogen  Nitrogen                                        ______________________________________                                         Found           62.17    8.83      3.83                                        Calculated for C.sub.20 H.sub.35 NO.sub.4 S                                                    62.30    9.15      3.63                                        ______________________________________                                    

EXAMPLE 27

13.3 parts of 2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol and 2.9 parts of hexamethylenediamine are heated at 150° C. for 24 hours. The cooled reaction product is then triturated with 40°-60° petroleum-ether and yields N-N'-[5-(2'-hydroxy-5'-methoxyphenyl)-5-methyl-hexanoic acid amide] of hexane-1,6-diamine m.p. 58°-60° C.

    ______________________________________                                                       Carbon Hydrogen  Nitrogen                                        ______________________________________                                         Found           69.72    9.62      4.48                                        Calculated for C.sub.34 H.sub.52 N.sub.2 O.sub.6                                               69.83    8.96      4.79                                        ______________________________________                                    

EXAMPLE 28

2.4 parts of 2,5-bis-(6'-hydroxy-2'-methyl-hex-2'-yl)-4-ethoxyphenol, (from example 16), in 15 parts benzene, are treated with 10 parts of acetyl chloride in 5 parts benzene. After storing overnight at room temperature, the benzene is removed and the residue, after short-path distillation at 0.7 mb, gives 2,5-bis-(6'-acetoxy-2'-methyl-hex-2'-yl)-4-ethoxyphenol as a pale yellow viscous oil.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             69.38   9.39                                                 Calculated for C.sub.26 H.sub.42 O.sub.6                                                         69.30   9.39                                                 ______________________________________                                    

EXAMPLE 29

(a) 4.3 parts of 3-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol (from example 10), 2.0 parts of isobutylene and 0.2 part of p-toluene sulphonic acid in 25 parts of benzene are sealed into a glass tube and heated at 100° C. for 40 hours. The cooled reaction mixture is diluted with ether, and the ether solution is washed with 2N sodium hydroxide and water. Evaporation of the ether and benzene gives 2-t-butyl-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol as a white crystalline solid, m.p. 71°-3° C. from 60°-80° C. petroleum ether.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             70.65   9.62                                                 Calculated for C.sub.19 H.sub.30 O.sub.4                                                         70.77   9.38                                                 ______________________________________                                    

(b) 2-t-butyl-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol from example 29a) is transesterified with n-hexanol by the procedure of example 3. Short-path distillation at 1 mb gives 2-t-butyl-5-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol as a pale yellow viscous oil with the following percentage composition by weight:

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             73.76   10.51                                                Calculated for C.sub.24 H.sub.40 O.sub.4                                                         73.43   10.27                                                ______________________________________                                    

EXAMPLE 30

(a) 2-cumyl-5-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol m.p. 102°-4° C. from petroleum ether, is obtained from alphamethyl styrene and 3-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol by the procedure of example 29.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             75.21   8.49                                                 Calculated for C.sub.24 H.sub.32 O.sub.4                                                         74.97   8.39                                                 ______________________________________                                    

(b) 2-cumyl-5-(5'-n-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-4-methoxyphenol is obtained by transesterification of the methyl ester from example 30a) with n-hexanol using the procedure of example 3, and is obtained as a pale yellow viscous oil after short-path distillation at 0.7 mb.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             76.62   9.21                                                 Calculated for C.sub.29 H.sub.42 O.sub.4                                                         76.61   9.31                                                 ______________________________________                                    

EXAMPLE 31

2.5 parts of 2-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-hydroquinone, 0.68 part isoprene, 0.1 part p-toluene sulphonic acid and 15 parts benzene are sealed into a glass tube and heated at 80° C. for 3 days. The product is worked up as in example 13 and gives 6-hydroxy-7-(5'-methoxycarbonyl-2'-methyl-pent-2'-yl)-2,2-dimethylchroman as a pale yellow oil after short-path distillation at 0.7 mb

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             71.44   8.84                                                 Calculated for C.sub.19 H.sub.28 O.sub.4                                                         71.22   8.81                                                 ______________________________________                                    

USE EXAMPLE 1

0.05 mMol of the magenta coupler of the following formula ##STR36## and 0.025 mMol of the compound of formula I are dissolved in 2.0 ml of tricresylphosphate/ethyl acetate (0.75 g/100 ml). 7.0 ml of a 6% gelatin solution, 1.0 ml of a 0.8% solution of the wetting agent of the formula ##STR37## are put into water, then emulsified for 5 minutes by means of a 100-Watt ultra-sonic appliance. 2.5 ml of coupler-additive emulsion, freshly treated in the ultra-sonic appliance, 2.0 ml of silver bromide emulsion with a content of 0.6% silver, 0.7 ml of a 1% aqueous solution of the curing agent with the following formula ##STR38## and 2.8 ml of water are mixed together, set to a pH value of 6.5, and at 40° C. poured onto a polyethylene paper measuring 14×18 cm. After the coating has hardened at 10° C., the poured-on mixture is dried at room-temperature.

Processing

The samples of the coated paper obtained are exposed to light of 500 Lux under a step-wedge for 6 seconds and then processed as follows at 32.8° C. (±0.3° C.):

    ______________________________________                                         1. Developer bath 3.5 minutes                                                  2. Bleaching fixing bath                                                                         1.5 minutes                                                  3. Washing        3.0 minutes                                                  4. Drying         1.0 minutes                                                  ______________________________________                                    

The developer bath has the following composition:

    ______________________________________                                         4-amino-3-methyl-N--ethyl-N--[β-(methyl-sulphonamido)                     ethyl]-aniline                                                                 11/2 H.sub.2 SO.sub.4.H.sub.2 O                                                                     4.85   (g/liter)                                          Potassium bromide    0.6                                                       Potassium carbonate  32.0                                                      Lithium sulphate     1.8                                                       Potassium sulphite   2.0                                                       Hydroxylaminesulphite                                                                               3.9                                                       Ethyleneglycol       21.3                                                      Benzyl alcohol       15.1                                                      Water                to 1   liter                                              ______________________________________                                    

The pH value is 10.1

The bleaching fixing bath used is a conventional bath, with e.g. the following composition:

    ______________________________________                                         Ammoniumthiosulphate (80% solution)                                                                    200    (g/liter)                                       Sodium sulphite (anhydrous)                                                                            15                                                     Sodium carbonate (anhydrous)                                                                           2.5                                                    Ethylenediamine tetra-acetic acid,                                                                     2                                                      sodium salt                                                                    Ethylenediamine tetra-acetic acid                                                                      50                                                     sodium-iron-(III)-salt                                                         Water                   to 1   liter                                           ______________________________________                                    

After washing and drying, clear, sharp magenta wedges are obtained with absorption maximum at 537 nm and maximum reflectance densities of 1.80.

A step-wedge obtained in this way is illuminated in an Atlas weather ometer (2500 W lamp) with a total energy of 42 kJ/cm² through an ultra-violet filter (Kodak Wratten 2C). For comparison, a step-wedge prepared analogously, which contains no compound according to the invention, is used.

In all cases the residual optional density (OD) was measured in % of the initial density (initial density 1.0). Table 1 contains the results.

                  TABLE 1                                                          ______________________________________                                         Light Stabilizing Effect of Compounds of Formula I                             compound of formula I,                                                         product of   % OD (with UV filter; 42 kJ/cm.sup.2)                             ______________________________________                                         none         47                                                                Example 1a   86                                                                Example 3    90                                                                Example 4    90                                                                Example 5    85                                                                Example 6a   85                                                                Example 7    86                                                                Example 8    90                                                                Example 9a   88                                                                Example 9c   89                                                                Example 13   91                                                                ______________________________________                                    

Compared with the emulsion without stabiliser, emulsions containing the compounds of formula I are more stable to light.

USE EXAMPLE 2

A coating is prepared according to Use Example 1, which contains 0.0125 mMol of the compound of Example 3 and 0.0125 mMol of the compound of formula A ##STR39## instead of 0.025 mMol of one of the products of the Examples 1 to 5, and exposed, processed and illuminated as described in Use Example 1. The remaining density is 89 percent of an original density of 1.0.

The compound of formula A is prepared as follows:

5.5 Parts of hydroquinone, 21.2 parts of n-hexyl 5-methyl-hex-5-enoate, and 1.0 parts of p-toluene sulphonic acid are heated on a steam-bath for 4 days. The cooled reaction mixture is taken up in ether, washed with 10% sodium hydroxide solution and then with water, until neutral. After stripping, the residual oil which partially solidifies, is triturated with 40°-60° petroleum ether and gives 2,5-bis-(5'-hexyloxycarbonyl-2'-methyl-pent-2'-yl)-hydroquinone m.p. 77°-8° C. A further crystallisation from 60°-80° petroleum ether gives material m.p. 83°-6° C.

    ______________________________________                                                         Carbon                                                                               Hydrogen                                                 ______________________________________                                         Found             71.77   10.23                                                Calculated for C.sub.32 H.sub.54 O.sub.6                                                         71.87   10.18                                                ______________________________________                                    

USE EXAMPLE 3

Coatings are produced according to Use Example 1 with a molar coupler to stabilizer ratio of 2:1 and exposed through a Kodak Photographic Step Tablet No. 2. Table 2 contains the green reflectance densities of the steps No. 3, 5 and 7.

                  TABLE 2                                                          ______________________________________                                         Dye yield in the presence of substituted hydroquinone ethers                            Reflectance density                                                   Product    step 3       step 5  step 7                                         ______________________________________                                         none       52           90      134                                            Example 1a 51           94      138                                            Example 7  53           91      142                                            Example 8  51           88      132                                            ______________________________________                                    

It can be clearly seen that the products of the invention have no influence on dye yield.

USE EXAMPLE 4

In an analogous series of experiments to those described in Use Example 1 a further compound of formula I is evaluated and the result given in Table 3.

                  TABLE 3                                                          ______________________________________                                         Light stabilizing effect of the compound of Example 12                         Compound of Formula I                                                                          % OD (with UV filter;                                          Hydroquinone Ether                                                                             42 kJ/cm.sup.2)                                                ______________________________________                                         Without light stabilizer                                                                       45                                                             Product of Example 12                                                                          83                                                             ______________________________________                                     

What is claimed is:
 1. A colour photographic silver halide material on a support which comprises at least one colour coupler--containing silver halide emulsion layer, there being present in the silver halide emulsion layer(s) or in a layer adjacent to the silver halide emulsion layer(s) a light stabilising amount of at least one compound having the formula I ##STR40## wherein p is 1 or 2 and q is 0 or 1, provided that p+q is 1 or 2; R is a residue of formula II ##STR41## wherein Q is selected from the residues: (i) --COZR₄ wherein Z is --O-- or ##STR42## and R₄ independently is --H, a C₁ -C₂₀ straight or branched chain alkyl optionally interrupted by 1 to five oxygen atoms and optionally substituted by a group --OR₆ wherein R₆ is C₃ -C₁₂ cycloalkyl, straight or branched C₃ -C₂₀ alkenyl, C₆ -C₁₀ aryl optionally substituted by one or two C₁ -C₄ alkyl groups or C₇ -C₁₃ aralkyl, or R₄ is a C₂ -C₂₀ divalent straight or branched chain alkylene residue, a C₃ -C₂₀ straight or branched chain alkenyl group or a C₃ -C₁₂ cycloalkyl group; a C₆ -C₁₀ aryl group optionally substituted by one or two C₁ -C₈ alkyl groups or a C₇ -C₁₃ aralkyl group; a 5 or 6 membered heterocycle containing an oxygen atom, and optionally substituted by one or two C₁ -C₄ straight or branched chain alkyl groups; or methyl substituted by a 5 or 6 membered heterocycle containing an oxygen atom and optionally substituted by one or two C₁ -C₄ straight or branched chain alkyl groups; and when Z is --NR₅, R₅ is hydrogen or a straight or branched chain C₁ -C₂₀ alkyl group or a C₅ -C₆ cycloalkyl group, or R₄ and R₅ together with the nitrogen atom to which they are each bonded may form a 5 or 6 membered heterocyclic ring, optionally substituted by one or two C₁ -C₄ alkyl groups;(ii) --OX wherein X is R₇ or --COR₇, wherein R₇ is --H or a C₁ -C₂₀ straight or branched chain alkyl group, a C₃ -C₂₀ straight or branched chain alkenyl group, a C₃ -C₁₂ cycloalkyl group, a C₇ -C₁₃ alkyl group, or a C₆ -C₁₀ aryl group, optionally substituted by one or two C₁ -C₄ alkyl groups; (iii) --N(R₈)(R₉) wherein R₈ and R₉ independently, are --H or a C₁ -C₂₀ straight or branched chain alkyl group, a C₃ -C₂₀ straight or branched chain alkenyl group, a C₃ -C₁₂ cycloalkyl group, a C₇ -C₁₃ aralkyl group or a C₆ -C₁₀ aryl group optionally substituted by one or two C₁ -C₄ alkyl groups, or an acyl group of formula --COR₇ wherein R₇ has its previous significance, or R₈ and R₉, together with the nitrogen atom to which they are each bonded, form a 5- or 6-membered heterocyclic ring, optionally substituted by one or two C₁ -C₄ alkyl groups; (iv) --PO(OR₁₀)([O]_(x) R₁₁) wherein x is 0 or 1, and when x is 1 R₁₀ and R₁₁ are the same or different and each is --H or a straight or branched chain C₁ -C₂₀ alkyl group, or a C₆ -C₁₀ aryl optionally substituted with one or two C₁ -C₄ alkyl groups; or R₁₀ and R₁₁ may be linked together to form a C₂ -C₃ alkylene chain optionally substituted by one to four C₁ -C₂₀ alkyl groups; and when x is 0, R₁₀ has its previous significance and R₁₁ is a C₁ -C₅ straight chain alkyl group; (v) --SO₂ R₁₂ wherein R₁₂ is --OH, --Cl or --N(R₅)(R₇) wherein R₅ and R₇ have their previous significance; provided that, when R₁₂ is --OH, then R₁ is a residue of formula II; (vi) --CN, halogen or --NO₂ ; and (vii) --COR₁₅ wherein R₁₅ is --H or a C₁ -C₂₀ straight or branched chain alkyl group or halogen; n is an integer from 1 to 20; k is 1 or 2; R₂ and R₃ are the same or different and each is straight or branched chain alkyl group having from 1 to 5 carbon atoms and, when Q is --CO₂ R₄, either R₂ or R₃ is optionally substituted by a --CO₂ R₄ group, the R₄ groups being independent, or when Q is --COOR₄ R₂ or R₃ may be so linked to the residue C_(n) H_(2n) --COOR₄ that there is formed a C₅ -C₁₂ cycloalkylene residue optionally substituted by another group --CO₂ R₄ the R₄ groups being independent, wherein R₄ has its previous significance; or when Q is --COR₁₅, R₂ and R₃ may be so linked to the residue C_(n) H_(2n) --COR₁₅ that there is formed a C₅ -C₁₂ cycloalkylene residue wherein R₁₅ has its previous significance; provided that, when the group Q is a --CO₂ R₄ residue wherein R₄ is a C₂ -C₂₀ divalent straight or branched chain alkylene residue then p and k are both 1 and the compound of formula I has the formula Ia: ##STR43## wherein R₄₀ is a C₂ -C₂₀ divalent straight or branched chain alkylene residue; and provided that, when the group Q is a --CON(R₄)(R₅) residue wherein R₄ is a C₂ -C₂₀ divalent straight or branched chain alkylene residue and R₅ has its previous significance, then p and k are both 1 and the compound of formula I has the formula Ib: ##STR44## wherein R₂, R₃, q and n have their previous significance, R₄₁ is a C₂ -C₂₀ divalent straight or branched chain alkyl residue; R₁ is C₁ -C₈ straight or branched chain alkyl, C₅ -C₇ cycloalkyl optionally substituted by one or two methyl or ethyl groups, C₇ -C₉ aralkyl or a residue of formula II as hereinbefore defined, and when R₁ is a residue of formula II then R₁ and R may be the same or different; or R₁ is a residue of formula III: ##STR45## in which R and p have their previous significance; and M is a direct bond; --C(R₁₃)(R₁₄)-- in which R₁₃ and R₁₄ are the same or different and are hydrogen, C₁ -C₂₀ straight or branched chain alkyl optionally interrupted by 1 to 3 sulphur atoms, C₆ -C₁₀ aryl or R₁₃ and R₁₄, together with the carbon atom to which they are attached may form a 5- or 6-membered ring which may be further substituted by one or two C₁ -C₈ straight or branched chain alkyl groups; --S--; --S--S--; --SO₂ --; --CH₂ SCH₂ --; --CH₂ OCH₂ -- or --C(CH₃)₂ -p-phenylen-C(CH₃)₂ --; R_(o) and R_(oo) are the same or different and each is hydrogen, a C₁ -C₂₀ straight or branched chain alkyl group optionally interrupted by 1 to 5 oxygen atoms, a C₃ -C₁₂ cycloalkyl group, a C₆ -C₁₀ aryl group optionally substituted by one or two C₁ -C₄ straight or branched chain alkyl groups, or a C₇ -C₁₃ aralkyl group provided that both of R_(o) and R_(oo) are not hydrogen, or R_(oo) has its previous significance and R_(o) is a residue of formula IV: ##STR46## in which R, R_(oo), R₁ and q have their previous significance, or R_(o) and R₁, when in ortho position to one another, together with the carbon atoms to which they are attached, may form an optionally substituted residue of formula V: ##STR47## wherein A is a carbon residue containing 4 to 20 carbon atoms which forms a substituted chroman or coumaran system, or R_(o) and R₁ together may form a residue having the formula VI or VII: ##STR48## wherein R, R_(o) and R_(oo) have their previous significance, provided that the compound of formula I contains only one residue of formula III or IV; or R_(oo) is hydrogen and R_(o) is a residue having the formula IVa or IVb: ##STR49## wherein p, q and R have their previous significance, R₁ " is C₁ -C₈ straight or branched alkyl, C₇ -C₉ aralkyl or a residue of formula II, as hereinbefore defined, m is 1 or 2, B, when m is 1, represents C₂ -C₁₂ alkylene which may be interrupted by 1 to 3 oxygen or sulphur atoms, C₄ -C₁₀ alkenylene, C₅ -C₁₂ cycloalkylene, C₆ -C₁₂ arylene, C₈ -C₁₂ aralkylene, C₄₋₆ alkynylene, xylylene, --CH₂ CH(OH)CH₂ --, --CH₂ CH(OH)CH₂ --O--Y--O--CH₂ CH(OH)CH₂ --, ##STR50## or --CH₂ COO--B'--OCOCH₂ -- wherein Y is C₂ -C₁₀ alkylene, C₆ -C₁₂ arylene, ##STR51## or C₆ -C₁₂ cycloalkylene, B' is C₂ -C₈ alkylene, C₄ -C₈ oxaalkylene, or cyclohexylene and, when m is 2, B represents a group of the formula ##STR52## r is 0 to 12, R₁₆ represents hydrogen or straight or branched C₁ -C₁₂ alkyl and D is --OR₄ or --N(R₄)(R₅) wherein R₄ and R₅ have their previous significance; and with the proviso that excluded from the scope of the claim are those compounds in which p is 1, q is 1, Q is COR₁₅ wherein R₁₅ is H, R_(o) and R_(oo) are C₁ -C₂₀ alkyl and R₁ is C₁ -C₈ alkyl, as well as salts of compounds of formula I with bases or organic or inorganic acids, respectively, when Q is an acidic or basic group.
 2. Photographic material according to claim 1 wherein a further organic stabiliser, UV absorber, optical brightening agent, antifogging agent, and/or plasticizer are also present.
 3. Photographic material according to claim 2 wherein the further organic stabiliser is a hydroquinone compound of formula XII ##STR53## wherein R₁ is C₁ -C₈ alkyl, C₇ -C₉ aralkyl or a residue of formula II or III as defined in claim 2 and R, p and q are as defined in claim
 2. 